What critical information should be included in a compounded product's record?

In the context of compounding pharmacy, maintaining accurate and comprehensive records is essential for ensuring the safety, efficacy, and traceability of compounded products. Including the manufacturer and lot number of each ingredient in a compounded product's record is critical for several reasons.

First, the lot number helps to identify the specific batch of the ingredient that was used in the compounding process. This information is vital in the event that there is a recall or a safety issue associated with that particular batch. Being able to trace back to the exact lot number allows pharmacists to take appropriate actions to protect patients and ensure drug safety.

Second, knowing the manufacturer adds an additional layer of accountability and quality assurance. Different manufacturers may have different standards of quality, and understanding which manufacturer provided the ingredients can help pharmacists assess potential variability in efficacy or safety.

Maintaining this information in the compounded product's record not only complies with legal and regulatory requirements but also supports good compounding practices that promote patient safety. This level of detail is crucial should any questions arise regarding the compounded product's ingredients or integrity later on.